FI812326L - THERMAL SUBSTANCES FOR IMMEDIATE PHARMACEUTICALS FOR PHARMACEUTICALS - Google Patents

THERMAL SUBSTANCES FOR IMMEDIATE PHARMACEUTICALS FOR PHARMACEUTICALS

Info

Publication number
FI812326L
FI812326L FI812326A FI812326A FI812326L FI 812326 L FI812326 L FI 812326L FI 812326 A FI812326 A FI 812326A FI 812326 A FI812326 A FI 812326A FI 812326 L FI812326 L FI 812326L
Authority
FI
Finland
Prior art keywords
pharmaceuticals
immediate
thermal substances
substances
thermal
Prior art date
Application number
FI812326A
Other languages
Finnish (fi)
Inventor
Alfred Sallmann
Original Assignee
Ciba Geigy Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag
Publication of FI812326L publication Critical patent/FI812326L/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/53—Nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/46—Oxygen atoms
    • C07D213/50—Ketonic radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/26—Radicals substituted by carbon atoms having three bonds to hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
FI812326A 1980-07-25 1981-07-24 THERMAL SUBSTANCES FOR IMMEDIATE PHARMACEUTICALS FOR PHARMACEUTICALS FI812326L (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH571580 1980-07-25

Publications (1)

Publication Number Publication Date
FI812326L true FI812326L (en) 1982-01-26

Family

ID=4298165

Family Applications (1)

Application Number Title Priority Date Filing Date
FI812326A FI812326L (en) 1980-07-25 1981-07-24 THERMAL SUBSTANCES FOR IMMEDIATE PHARMACEUTICALS FOR PHARMACEUTICALS

Country Status (23)

Country Link
US (1) US4447431A (en)
EP (1) EP0045081B1 (en)
JP (1) JPS5756466A (en)
KR (13) KR850000883B1 (en)
AR (1) AR230269A1 (en)
AT (1) ATE17349T1 (en)
AU (2) AU7340481A (en)
CA (1) CA1175431A (en)
DD (2) DD201677A5 (en)
DE (1) DE3173434D1 (en)
DK (1) DK331881A (en)
ES (8) ES504257A0 (en)
FI (1) FI812326L (en)
GB (1) GB2080805B (en)
GR (1) GR75287B (en)
IE (1) IE52071B1 (en)
IL (1) IL63410A (en)
NO (1) NO812542L (en)
NZ (1) NZ197828A (en)
PL (8) PL236997A1 (en)
PT (1) PT73424B (en)
SU (8) SU1235454A3 (en)
ZA (1) ZA815078B (en)

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GB2123831B (en) * 1981-07-20 1986-01-15 Ciba Geigy Ag Trisubstituted oxazo compounds
EP0084756A1 (en) * 1982-01-22 1983-08-03 Ciba-Geigy Ag Trisubstituted oxaza compounds
FR2633291B1 (en) * 1988-06-27 1990-09-07 Oreal 4-HYDROXY ISOXAZOL DERIVATIVES, THEIR PREPARATION PROCESS AND COSMETIC AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US5252322A (en) * 1989-09-22 1993-10-12 The Gillette Company Skin tanning compositions containing imidazoles
NZ239161A (en) * 1990-07-31 1994-01-26 Smithkline Beecham Corp Substituted [1h-imidazol-5-yl] alkanoic acid derivatives; medicaments,
US5916891A (en) 1992-01-13 1999-06-29 Smithkline Beecham Corporation Pyrimidinyl imidazoles
IL104369A0 (en) * 1992-01-13 1993-05-13 Smithkline Beecham Corp Novel compounds and compositions
US5670527A (en) * 1993-07-16 1997-09-23 Smithkline Beecham Corporation Pyridyl imidazole compounds and compositions
US5593991A (en) * 1993-07-16 1997-01-14 Adams; Jerry L. Imidazole compounds, use and process of making
US5593992A (en) * 1993-07-16 1997-01-14 Smithkline Beecham Corporation Compounds
EP1306377A3 (en) * 1993-11-08 2003-05-07 Smithkline Beecham Corporation Pyridyl-oxazoles and their use as cytokines inhibitors
US5723477A (en) * 1994-11-10 1998-03-03 Sibia Neurosciences, Inc. Modulators of acetylcholine receptors
US5658903A (en) * 1995-06-07 1997-08-19 Smithkline Beecham Corporation Imidazole compounds, compositions and use
US5739143A (en) * 1995-06-07 1998-04-14 Smithkline Beecham Corporation Imidazole compounds and compositions
US6369068B1 (en) 1995-06-07 2002-04-09 Smithkline Beecham Corporation Amino substituted pyrimidine containing compounds
ZA9610687B (en) 1995-12-22 1997-09-29 Smithkline Beecham Corp Novel synthesis.
US6046208A (en) * 1996-01-11 2000-04-04 Smithkline Beecham Corporation Substituted imidazole compounds
AP9700912A0 (en) 1996-01-11 1997-01-31 Smithkline Beecham Corp Novel cycloalkyl substituted imidazoles
NZ327044A (en) * 1996-01-11 2000-01-28 Smithkline Beecham Corp Substituted imidazole compounds
ZA97175B (en) * 1996-01-11 1997-11-04 Smithkline Beecham Corp Novel substituted imidazole compounds.
JP2000507558A (en) * 1996-03-25 2000-06-20 スミスクライン・ビーチャム・コーポレイション Novel treatment for CNS injury
WO1998007425A1 (en) 1996-08-21 1998-02-26 Smithkline Beecham Corporation Imidazole compounds, compositions and use
US5929076A (en) * 1997-01-10 1999-07-27 Smithkline Beecham Corporation Cycloalkyl substituted imidazoles
UA65572C2 (en) * 1997-04-24 2004-04-15 Ortho Mcneil Pharm Inc Substituted imidazoles, intermediate compounds for the preparation thereof, a method for the preparation of substituted imidazoles and a method for the treatment of inflammatory diseases
JP2002504909A (en) 1997-06-13 2002-02-12 スミスクライン・ビーチャム・コーポレイション New substituted pyrazole and pyrazoline compounds
EP0994870A4 (en) 1997-06-19 2002-10-23 Smithkline Beecham Novel aryloxy substituted pyrimidine imidazole compounds
US6489325B1 (en) 1998-07-01 2002-12-03 Smithkline Beecham Corporation Substituted imidazole compounds
TW517055B (en) 1997-07-02 2003-01-11 Smithkline Beecham Corp Novel substituted imidazole compounds
AR016294A1 (en) * 1997-07-02 2001-07-04 Smithkline Beecham Corp IMIDAZOL SUBSTITUTE COMPOSITE, PHARMACEUTICAL COMPOSITION CONTAINING IT, ITS USE IN THE MANUFACTURE OF A MEDICINAL PRODUCT AND PROCEDURE FOR SUPREPARATION
US6562832B1 (en) 1997-07-02 2003-05-13 Smithkline Beecham Corporation Substituted imidazole compounds
US7301021B2 (en) * 1997-07-02 2007-11-27 Smithkline Beecham Corporation Substituted imidazole compounds
WO1999001452A1 (en) 1997-07-02 1999-01-14 Smithkline Beecham Corporation Novel cycloalkyl substituted imidazoles
US6362193B1 (en) 1997-10-08 2002-03-26 Smithkline Beecham Corporation Cycloalkenyl substituted compounds
WO1999032121A1 (en) 1997-12-19 1999-07-01 Smithkline Beecham Corporation Compounds of heteroaryl substituted imidazole, their pharmaceutical compositions and uses
TR200003472T2 (en) * 1998-05-22 2001-09-21 Smithkline Beecham Corporation New 2-alkyl substituted imidazole compounds
US6858617B2 (en) 1998-05-26 2005-02-22 Smithkline Beecham Corporation Substituted imidazole compounds
EP1112070B1 (en) * 1998-08-20 2004-05-12 Smithkline Beecham Corporation Novel substituted triazole compounds
AU1909200A (en) * 1998-11-04 2000-05-22 Smithkline Beecham Corporation Pyridin-4-yl or pyrimidin-4-yl substituted pyrazines
WO2000029399A1 (en) * 1998-11-12 2000-05-25 Boehringer Ingelheim (Canada) Ltd. Antiherpes compounds
US6239279B1 (en) 1998-12-16 2001-05-29 Smithkline Beecham Corporation Synthesis for 4-aryl-5-pyrimidine imidazole substituted derivatives
AU1623601A (en) 1999-11-22 2001-06-04 Smithkline Beecham Plc Novel compounds
US6759410B1 (en) * 1999-11-23 2004-07-06 Smithline Beecham Corporation 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors
DE60020595T2 (en) 1999-11-23 2006-03-16 Smithkline Beecham Corp. 3,4-DIHYDRO- (1H) CHINAZOLIN-2-ON COMPOUNDS AS CSBP / P38 KINASE INHIBITORS
ATE305787T1 (en) 1999-11-23 2005-10-15 Smithkline Beecham Corp 3,4-DIHYDRO-(1H)CHINAZOLINE-2-ONE COMPOUNDS AS CSBP/P39 KINASE INHIBITORS
AU1781601A (en) 1999-11-23 2001-06-04 Smithkline Beecham Corporation 3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors
US7235551B2 (en) * 2000-03-02 2007-06-26 Smithkline Beecham Corporation 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
ES2218391T3 (en) * 2000-03-06 2004-11-16 Smithkline Beecham Plc IMIDAZOL DERIVATIVES AS RAF-CINASA INHIBITORS.
GB0005357D0 (en) 2000-03-06 2000-04-26 Smithkline Beecham Plc Compounds
CZ20031125A3 (en) * 2000-10-23 2003-10-15 Smithkline Beecham Corporation Novel compounds
GB0112348D0 (en) * 2001-05-19 2001-07-11 Smithkline Beecham Plc Compounds
WO2003022837A1 (en) * 2001-09-05 2003-03-20 Smithkline Beecham P.L.C. Heterocycle-carboxamide derivatives as raf kinase inhibitors
TW200505446A (en) * 2003-01-17 2005-02-16 Fuj Isawa Pharmaceutical Co Ltd Inhibitor of cox
JP2006525320A (en) * 2003-05-08 2006-11-09 アステラス製薬株式会社 COX inhibitor
US7479558B2 (en) * 2005-03-25 2009-01-20 Glaxo Group Limited Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one derivatives
PE20100737A1 (en) 2005-03-25 2010-11-27 Glaxo Group Ltd NEW COMPOUNDS
WO2013049272A2 (en) 2011-09-29 2013-04-04 Theraceutix, Llc Composition and method for treatment of symptoms associated with various skin conditions

Family Cites Families (4)

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US3558645A (en) * 1968-07-08 1971-01-26 Sandoz Ag 2-(4-(4',5-diphenyl - 2 - imidazolyl)-phenoxy) lower aliphatic monocarboxylic acids
CH561202A5 (en) * 1971-05-10 1975-04-30 Ciba Geigy Ag
GB1469532A (en) * 1973-06-28 1977-04-06 Dumex Ltd As Imimdazolyl-alkanoic acid derivatives
US4372964A (en) * 1980-10-30 1983-02-08 E. I. Du Pont De Nemours And Company Antiinflammatory 4,5-diaryl-1H-imidazole-2-methanols

Also Published As

Publication number Publication date
NZ197828A (en) 1985-11-08
ES8301472A1 (en) 1982-12-01
SU1138023A3 (en) 1985-01-30
PL237004A1 (en) 1983-02-28
KR850001064B1 (en) 1985-07-25
DE3173434D1 (en) 1986-02-20
ES8306124A1 (en) 1983-05-16
KR850000873B1 (en) 1985-06-22
IE52071B1 (en) 1987-06-10
IL63410A0 (en) 1981-10-30
PL237003A1 (en) 1983-02-28
JPS5756466A (en) 1982-04-05
AU5655586A (en) 1986-09-11
KR850000892B1 (en) 1985-06-26
KR850002747A (en) 1985-05-15
ES514580A0 (en) 1983-05-16
IE811680L (en) 1982-01-25
SU1169534A3 (en) 1985-07-23
ES514584A0 (en) 1983-05-16
SU1205764A3 (en) 1986-01-15
KR850000891B1 (en) 1985-06-26
PL135822B1 (en) 1985-12-31
PL237005A1 (en) 1983-02-28
PL237000A1 (en) 1983-02-28
KR850002752A (en) 1985-05-15
ES8306123A1 (en) 1983-05-16
SU1235454A3 (en) 1986-05-30
DD202554A5 (en) 1983-09-21
AU7340481A (en) 1982-01-28
US4447431A (en) 1984-05-08
ES504257A0 (en) 1982-12-01
ES514582A0 (en) 1983-05-16
ES514583A0 (en) 1983-05-16
GB2080805A (en) 1982-02-10
KR850000885B1 (en) 1985-06-26
ATE17349T1 (en) 1986-01-15
ES8306120A1 (en) 1983-05-16
SU1205763A3 (en) 1986-01-15
KR850000884B1 (en) 1985-06-26
PT73424B (en) 1983-06-20
KR850002750A (en) 1985-05-15
EP0045081A3 (en) 1982-04-07
GR75287B (en) 1984-07-13
KR850000888B1 (en) 1985-06-26
CA1175431A (en) 1984-10-02
KR850002754A (en) 1985-05-15
KR850002753A (en) 1985-05-15
KR850002756A (en) 1985-05-15
KR850000890B1 (en) 1985-06-26
PL237002A1 (en) 1983-02-28
AR230269A1 (en) 1984-03-01
PL237001A1 (en) 1983-02-28
NO812542L (en) 1982-01-26
KR850002745A (en) 1985-05-15
SU1152520A3 (en) 1985-04-23
EP0045081B1 (en) 1986-01-08
DK331881A (en) 1982-01-26
KR830006230A (en) 1983-09-20
KR850002748A (en) 1985-05-15
ES8306121A1 (en) 1983-05-16
IL63410A (en) 1986-04-29
ZA815078B (en) 1982-07-28
ES8306119A1 (en) 1983-05-16
PL236997A1 (en) 1983-01-03
SU1227112A3 (en) 1986-04-23
ES514579A0 (en) 1983-05-16
SU1145928A3 (en) 1985-03-15
KR850000889B1 (en) 1985-06-26
PL232352A1 (en) 1982-12-20
KR850002749A (en) 1985-05-15
KR850002744A (en) 1985-05-15
KR850000887B1 (en) 1985-06-26
ES8306122A1 (en) 1983-05-16
DD201677A5 (en) 1983-08-03
KR850002755A (en) 1985-05-15
KR850000886B1 (en) 1985-06-26
PT73424A (en) 1981-08-01
GB2080805B (en) 1984-03-07
EP0045081A2 (en) 1982-02-03
ES514585A0 (en) 1983-07-01
ES8307245A1 (en) 1983-07-01
KR850000883B1 (en) 1985-06-26
ES514581A0 (en) 1983-05-16
KR850002746A (en) 1985-05-15
KR850000911B1 (en) 1985-06-27

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